Citation: Zhang Jingjing, Yao Ming, Li Li, Sang Dayong, Xiong Hangxing, Liu Shengpeng. Synthesis of Resveratrol, Piceatannol and Pinosylvin[J]. Chinese Journal of Organic Chemistry, ;2020, 40(4): 1062-1067. doi: 10.6023/cjoc201908014 shu

Synthesis of Resveratrol, Piceatannol and Pinosylvin

Zhang Jingjing ^a,b ,
Yao Ming ^b,, ,
Li Li ^a,b ,
Sang Dayong ^b ,
Xiong Hangxing ^a,b,, ,
Liu Shengpeng ^a,,

a.
School of Chemical Engineering and Pharmacy, Wuhan Institute of Technology, Wuhan 430205
b.
College of Chemical Engineering and Pharmacy, Jingchu University of Technology, Jingmen 448000

Corresponding author: Yao Ming, yaomingcep@jcut.edu.cn Xiong Hangxing, 731990153@qq.com Liu Shengpeng, liuabss@163.com
Received Date: 9 August 2019
Revised Date: 8 October 2019
Available Online: 2 December 2019
Fund Project: Project supported by the Science Technology Foundation for Creative Research Group of Hubei Department of Education (No. T201719)the Science Technology Foundation for Creative Research Group of Hubei Department of Education T201719

Figures(6)

A convenient method for the practical synthesis of resveratrol, piceatannol and pinosylvin is described. Resveratrol, pinosylvin and piceatannol can be achieved through a simultaneous demethylation and isomerization process from stilbenes with the aid of aluminum and iodine. The overall yields of the reaction were 68%, 78% and 56% (based on aromatic aldehyde). The solvent of the reaction can be reused after filtered. At the same time, quantum chemical calculations and control experiments show that iodine radical may be the key factor leading to cis-trans isomerization of double bond in the process of demethylation.
- resveratrol,
- stilbene,
- demethylation,
- Wittig reaction,
- cis-trans isomerisation
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